Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 10:112956367 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs28633840, rs59806607

This variant has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts and has 1 sample genotype.

Variant displays